Nitroalkane oxidase, a carbanion-forming flavoprotein homologous to acyl-CoA dehydrogenase

被引:42
作者
Fitzpatrick, PF [1 ]
Orville, AM
Nagpal, A
Valley, MP
机构
[1] Texas A&M Univ, Dept Biochem & Biophys, College Stn, TX 77843 USA
[2] Georgia Inst Technol, Sch Chem & Biochem, Atlanta, GA 30332 USA
关键词
flavoprotein nitroalkane oxidase; Acyl-CoA dchydrogenase; Acyl-CoA oxidase; structure; mechanism;
D O I
10.1016/j.abb.2004.08.021
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
While several flavoproteins will oxidize nitroalkanes in addition to their physiological substrates, nitroalkane oxidase (NAO) is the only one which does not require the anionic nitroalkane. This, in addition to the induction of NAO by nitroethane seen in Fusarium oxysporum, suggests that oxidation of a nitroaliphatic species is the physiological role of the enzyme. Mechanistic studies of the reaction with nitroethane as substrate have established many of the details of the enzymatic reaction. The enzyme is unique in being the only flavoprotein to date for which a carbanion is definitively established as an intermediate in catalysis. Recent structural analyses show that NAO is homologous to the acyl-CoA dehydrogenase and acyl-CoA oxidase families of enzymes. In NAO, the glutamate which acts as the active site base in the latter enzymes is replaced by an aspartate. (C) 2004 Elsevier Inc. All rights reserved.
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页码:157 / 165
页数:9
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